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ACTIVE NOT RECRUITING Phase 1

BGB-290 and Temozolomide in Treating Isocitrate Dehydrogenase (IDH)1/2-Mutant Grade I-IV Gliomas

NCT03749187 · View on ClinicalTrials.gov ↗

Study Summary

This phase I trial studies the side effects and best dose of BGB-290 and temozolomide in treating adolescents and young adults with IDH1/2-mutant grade I-IV glioma that is newly diagnosed or has come back. BGB-290 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving BGB-290 and temozolomide may work better in treating adolescents and young adults with IDH1/2-mutant grade I-IV glioma.

Interventions

  • DRUG Temozolomide (TMZ)
  • DRUG PARP Inhibitor BGB-290

Study Locations (11)

California

  • Children's Hospital Los Angeles — Los Angeles
  • University of California, San Francisco — San Francisco

Connecticut

  • Yale University — New Haven

Maryland

  • Johns Hopkins University/Sidney Kimmel Cancer Center — Baltimore

Massachusetts

  • Dana-Farber Cancer Institute — Boston

Missouri

  • Washington University School of Medicine — St Louis

New Jersey

  • Joseph M. Sanzari Children's Hospital at Hackensack University Medical Center — Hackensack

North Carolina

  • Duke University Medical Center — Durham

Oregon

  • Oregon Health and Science University — Portland

Trial Details

FieldValue
Enrollment Target 78 participants
Start Date 2019-04-03
Est. Completion 2029-07-30
Phase Phase 1

Sponsor

University of California, San Francis

1,574 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03749187

The ClinicalTrials.gov registry entry for NCT03749187 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 78 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francis, which has 1,574 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 10 conditions, with Glioblastoma appearing as the primary indexed condition, and to 2 interventions — of which Temozolomide (TMZ) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03749187 reports 11 study locations spanning 10 distinct geographic areas — top geographies include California, Connecticut, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03749187 about?

NCT03749187 is a clinical study titled "BGB-290 and Temozolomide in Treating Isocitrate Dehydrogenase (IDH)1/2-Mutant Grade I-IV Gliomas". This phase I trial studies the side effects and best dose of BGB-290 and temozolomide in treating adolescents and young adults with IDH1/2-mutant grade I-IV glioma that is newly diagnosed or has come back. BGB-290 may stop the growth of tumor cells by blocking some of the enzymes needed for cell gro...

What is the current status of trial NCT03749187?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 78 participants. The study started on 2019-04-03. Estimated completion is 2029-07-30.

What conditions does trial NCT03749187 study?

This clinical trial studies the following conditions: Glioblastoma, Recurrent Glioblastoma, Malignant Glioma, Low Grade Glioma, WHO Grade III Glioma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03749187?

The interventions under investigation include: Temozolomide (TMZ) (DRUG), PARP Inhibitor BGB-290 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03749187?

This trial is sponsored by University of California, San Francis, which has 1,574 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03749187 being conducted?

This trial has 11 study locations across California, Connecticut, Maryland, Massachusetts, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial